Senior Clinical Research Associate
ICON · Frankfurt, Germany
The apply link worked recently (not employer-confirmed).
Role summary
This senior-level clinical research role involves overseeing trial monitoring activities across multiple sites to ensure protocol compliance, regulatory adherence, and data integrity. The position requires extensive CRA experience, strong leadership capabilities, and fluency in German and English, with approximately 60% travel expected. A bachelor's degree in a scientific or healthcare discipline is required.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Extensive clinical research associate experience with strong protocol and regulatory knowledge
- Ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software
- Fluent in German and English
- Willingness to travel approximately 60%
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, resolve issues, and provide operational support
- Collaborate with cross-functional teams on accurate data collection and reporting
- Train site staff and other CRAs to maintain high standards of trial conduct
- Build and maintain relationships with site personnel to ensure smooth trial operations
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.